Found 4 hits of ic50 for monomerid = 50194676 Target/Host
(Institution) | Ligand | Target/Host
Links | Ligand
Links | Trg + Lig
Links | Ki
nM | ΔG°
kJ/mole | IC50
nM | Kd
nM | EC50/IC50
nM | koff
s-1 | kon
M-1s-1 | pH | Temp
°C |
|---|
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM50194676
(1-(4-methyl-3-(2-(methylamino)quinazolin-6-yl)phen...)Show SMILES CNc1ncc2cc(ccc2n1)-c1cc(NC(=O)Nc2cccc(c2)C(F)(F)F)ccc1C Show InChI InChI=1S/C24H20F3N5O/c1-14-6-8-19(31-23(33)30-18-5-3-4-17(11-18)24(25,26)27)12-20(14)15-7-9-21-16(10-15)13-29-22(28-2)32-21/h3-13H,1-2H3,(H,28,29,32)(H2,30,31,33) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 5 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen, Inc.
Curated by ChEMBL
| Assay Description
Inhibition of p38-alpha by HTRF kinase assay |
J Med Chem 49: 5671-86 (2006)
Article DOI: 10.1021/jm0605482
BindingDB Entry DOI: 10.7270/Q29G5MFD |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50194676
(1-(4-methyl-3-(2-(methylamino)quinazolin-6-yl)phen...)Show SMILES CNc1ncc2cc(ccc2n1)-c1cc(NC(=O)Nc2cccc(c2)C(F)(F)F)ccc1C Show InChI InChI=1S/C24H20F3N5O/c1-14-6-8-19(31-23(33)30-18-5-3-4-17(11-18)24(25,26)27)12-20(14)15-7-9-21-16(10-15)13-29-22(28-2)32-21/h3-13H,1-2H3,(H,28,29,32)(H2,30,31,33) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 8 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen, Inc.
Curated by ChEMBL
| Assay Description
Inhibition of Lck by HTRF kinase assay |
J Med Chem 49: 5671-86 (2006)
Article DOI: 10.1021/jm0605482
BindingDB Entry DOI: 10.7270/Q29G5MFD |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50194676
(1-(4-methyl-3-(2-(methylamino)quinazolin-6-yl)phen...)Show SMILES CNc1ncc2cc(ccc2n1)-c1cc(NC(=O)Nc2cccc(c2)C(F)(F)F)ccc1C Show InChI InChI=1S/C24H20F3N5O/c1-14-6-8-19(31-23(33)30-18-5-3-4-17(11-18)24(25,26)27)12-20(14)15-7-9-21-16(10-15)13-29-22(28-2)32-21/h3-13H,1-2H3,(H,28,29,32)(H2,30,31,33) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 52 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen, Inc.
Curated by ChEMBL
| Assay Description
Inhibition of KDR by HTRF kinase assay |
J Med Chem 49: 5671-86 (2006)
Article DOI: 10.1021/jm0605482
BindingDB Entry DOI: 10.7270/Q29G5MFD |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase JAK3
(Homo sapiens (Human)) | BDBM50194676
(1-(4-methyl-3-(2-(methylamino)quinazolin-6-yl)phen...)Show SMILES CNc1ncc2cc(ccc2n1)-c1cc(NC(=O)Nc2cccc(c2)C(F)(F)F)ccc1C Show InChI InChI=1S/C24H20F3N5O/c1-14-6-8-19(31-23(33)30-18-5-3-4-17(11-18)24(25,26)27)12-20(14)15-7-9-21-16(10-15)13-29-22(28-2)32-21/h3-13H,1-2H3,(H,28,29,32)(H2,30,31,33) | PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 1.14E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen, Inc.
Curated by ChEMBL
| Assay Description
Inhibition of Jak3 by HTRF kinase assay |
J Med Chem 49: 5671-86 (2006)
Article DOI: 10.1021/jm0605482
BindingDB Entry DOI: 10.7270/Q29G5MFD |
More data for this
Ligand-Target Pair | |
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